FDA Inspection 1224183 — Eurofins Amatsi Analytics

Eurofins Amatsi Analytics — FEI 3006118993

The FDA completed an inspection of Eurofins Amatsi Analytics on November 3, 2023 in Fontenilles. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 3, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Fontenilles (France)

Additional Details

Bioanalytical BA/BE